MED-LOK SAFETY NEEDLE— 510(k) K103781

Substantially Equivalent

Sta-Med, LLC

FDA 510(k) clearance K103781 for MED-LOK SAFETY NEEDLE, Substantially Equivalent on 2011-02-08. Applicant: Sta-Med, LLC.

Clearance details

Applicant: Sta-Med, LLC
Product code: Code MEG
Advisory panel: General Hospital
Date received: 2010-12-27
Decision date: 2011-02-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Anaheim, CA, US

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Adverse events under product code MEG

product code MEG

Malfunction: 1,373
Other: 1
Total: 1,374

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.